In-Silico Structure Database (LMISSD)

Systematic Name
Galα1-3Galβ1-4GlcNAcβ1-3(Galα1-3Galβ1-4GlcNAcβ1-6)Galβ1-4GlcNAcβ1-3(GlcNAcβ1-6)Galβ1-4GlcNAcβ1-3Galβ1-4Glcβ-Cer(d18:1/18:0)
LM ID
LMSP0505BZ02
Status
Active (generated by computational methods)
Exact Mass
Calculate m/z
2877.362864
Formula

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MDLMOL SDF CSV TSV PNG
MDLMOL files can be opened in various drawing programs. In ChemDraw, open as filetype "MDL Molfile".

Main

Classification

Category
Main Class
Sub Class
Sphingolipids [SP]
Neutral glycosphingolipids [SP05]
Galbeta1-4GlcNAcbeta1-3Galbeta1-4Glc- (Neolacto series) [SP0505]

String Representations

InChiKey (Click to copy)
JSTOINALYCMQJQ-HQDOZQPMSA-N
InChi (Click to copy)
InChI=1S/C124H216N6O68/c1-8-10-12-14-16-18-20-22-23-25-27-29-31-33-35-37-72(148)130-57(58(147)36-34-32-30-28-26-24-21-19-17-15-13-11-9-2)49-173-117-96(167)93(164)106(69(48-141)186-117)193-122-97(168)107(81(152)62(41-134)181-122)194-114-75(127-54(5)144)89(160)104(67(46-139)183-114)191-123-100(171)110(84(155)70(187-123)50-174-112-73(125-52(3)142)86(157)78(149)59(38-131)176-112)195-116-77(129-56(7)146)90(161)105(68(47-140)185-116)192-124-101(172)111(196-115-76(128-55(6)145)88(159)103(66(45-138)184-115)190-121-99(170)109(83(154)64(43-136)180-121)198-119-95(166)92(163)80(151)61(40-133)178-119)85(156)71(188-124)51-175-113-74(126-53(4)143)87(158)102(65(44-137)182-113)189-120-98(169)108(82(153)63(42-135)179-120)197-118-94(165)91(162)79(150)60(39-132)177-118/h34,36,57-71,73-124,131-141,147,149-172H,8-33,35,37-51H2,1-7H3,(H,125,142)(H,126,143)(H,127,144)(H,128,145)(H,129,146)(H,130,148)/b36-34+/t57-,58+,59?,60?,61?,62?,63?,64?,65?,66?,67?,68?,69?,70?,71?,73?,74?,75?,76?,77?,78+,79-,80-,81-,82-,83-,84-,85-,86+,87+,88+,89+,90+,91-,92-,93+,94?,95?,96?,97?,98?,99?,100?,101?,102+,103+,104+,105+,106+,107-,108-,109-,110-,111-,112+,113+,114-,115-,116-,117+,118-,119?,120-,121-,122-,123-,124-/m0/s1
SMILES (Click to copy)
CC(=O)NC1[C@@H](O[C@@H]2[C@H](O)C(CO[C@H]3OC(CO)[C@H](O)[C@@H](O)C3NC(C)=O)O[C@H](O[C@H]3C(CO)O[C@H](O[C@H]4C(O)[C@H](OC(CO)[C@H]4O)O[C@H]4C(CO)O[C@H](OC[C@@H](NC(=O)CCCCCCCCCCCCCCCCC)[C@@H](O)/C=C/CCCCCCCCCCCCC)C(O)[C@@H]4O)C(NC(C)=O)[C@@H]3O)C2O)OC(CO)[C@H](O[C@H]2OC(CO[C@H]3OC(CO)[C@H](O[C@H]4OC(CO)[C@@H](O)[C@@H](O[C@H]5OC(CO)[C@@H](O)[C@@H](O)C5O)C4O)[C@@H](O)C3NC(C)=O)[C@@H](O)[C@@H](O[C@H]3OC(CO)[C@H](O[C@H]4OC(CO)[C@@H](O)[C@@H](O[C@@H]5OC(CO)[C@@H](O)[C@@H](O)C5O)C4O)[C@@H](O)C3NC(C)=O)C2O)[C@H]1O

References

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 198
Rings 13
Aromatic Rings 0
Rotatable Bonds 76
Van der Waals Molecular Volume 2638.32
Topological Polar Surface Area 1169.77
Hydrogen Bond Donors 42
Hydrogen Bond Acceptors 68
logP 5.95
Molar Refractivity 698.18